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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329410Generated: October 30, 2026

2-Furancarboxylic acid → 6-Fluoronaphthalene-1-carboxylic acid

https://huagongshe.com/reaction/329410

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Furancarboxylic acidHCID 6919—
ReactantFluorobenzeneHCID 10008—
CatalystAluminum(III) ChlorideHCID 6451240—
Product6-Fluoronaphthalene-1-carboxylic acidHCID 145813856.1%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a 1 liter round-bottomed flask equipped with condenser and N2 inlet were added 345 ml (3.68 mol) of fluorobenzene and 48 g (0.428 mol) of furoic acid. To the stirring suspension was added in portions 120 g (0.899 mmol of aluminum chloride. The reaction mixture was stirred at 95° C. for 16 hours and then quenched by addition to ice/water/1N HCl. After stirring 1 hour, the aqueous layer was decanted, and benzene and a saturated aqueous solution of sodium bicarbonate were added. After stirring 1 hour, the layers were separated, the aqueous layer washed with benzene, acidified, and extracted into ethyl acetate. The ethyl acetate layer was washed with water and brine, dried over sodium sulfate, and evaporated to a solid. The solid was triturated with isopropyl ether to give 5.0 g (6.1%) of a white solid, NMR (DMSO-d6): 7.0-8.0 (m, 5H), 8.6 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04891375
Source datasetuspto-grants-1990_01
ORD IDord-69a0858a28ce4c0fbaa8b5ce6928cd75
Source noteuspto-grants-1990_01